At Atlantic Analytical, we strive to give each customer the personalized attention they deserve, including direct
access to our technical specialists for advice or to answer any questions. "Priority Rush" service can be selected whenever immediate
results are necessary.
| News & Upcoming Exhibitions |
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Impurity Profiling Website Launched
May 2007
AAL has launched a new website
dedicated to our pharmaceutical Impurity Profiling services and expertise.
Click here for more information |
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EAS 2008
November 17, 18, 19, & 20
Garden State Convention Center
Somerset, NJ
Click here for more information |
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Our knowledge and experiences in gases and volatiles testing are diverse, yet highly specialized, with expertise in Gas Chromatography (GC),
Mass Spectrometry (MS), Gas Mass Spectrometry (Gas-MS) and Fourier Transform Infra Red (FTIR) methodology for high purity gas analysis from
the major gas chemicals and pharmaceutical producers; cryogenic air separation and impurity determination for Liquid Nitrogen (LIN), Liquid
Oxygen (LOX), Liquid Argon (LAR); semiconductors and integrated circuits for Residual Gas Analysis (RGA) by Mil-Std-883 Test Method 1018 and
outgassing/leak testing by Mass Spectrometry; pharmaceutical applications such as USP, EP and JP grade gases such as Nitrogen (by a comparable
yet superior Mass Spec method), Oxygen, Carbon Dioxide and Medicinal Air; headspace analysis and custom methods; natural and fuel gases; manufactured
synthetic gases; liquefied gases; Helium, Hydrogen and HyCO; beverage grade Carbon Dioxide; Air Analysis and Compressed Breathing Air for SCBA
and SCUBA applications.
Our pharmaceutical expertise continues to grow with the addition of a new cGMP facility specializing in developing and validating
analytical methods designed for reducing the quantitation limits for residual solvents, alkylating agents, genotoxins and reactive sulfurs
such as mesylates. We have also expanded our multi-compendial testing to now cover USP, EP and JP grade gases. In addition, we develop novel
small-scale small-molecule synthetic reagents, primary standards and chemical markers for pharmaceutical, biotechnology, clinical and contract
research organizations (CROs). These compounds can be with or without isotopic labeling, and come with complete structural information confirmed
by using the four (4) principal spectroscopic techniques, namely Mass Spectrometry (MS), Nuclear Magnetic Resonance (NMR), Infrared (IR) and
Ultraviolet/Visible (UV/VIS).
We comply with FDA, ISO/IEC 17025:2005, CGA, Mil. Spec, USP/NF, EP, ISBT, NFPA 99, and NFPA 1404 criteria, however our services go one step further. We also offer
both on-site sampling & testing programs. Clients that benefit from these services include: pharmaceuticals, cogeneration power plants,
manufacturing facilities, clinics, hospitals, companies concerned about indoor air quality or industrial hygiene, and landfill operators responsible
for emission compliance. We are ISO Accredited, FDA Inspected "without a 483 being issued", a “Suitable” laboratory for the Defense Supply Center Columbus (DSCC), and an “Approved” laboratory
for Coca-Cola™ and Pepsi™. We offer a comprehensive
package of analytical gas, volatiles and non-volatile impurities testing services to support your product development and marketed product activities. |
